A newly discovered bacterial defense protein named Cat1 reveals an extraordinary method of viral neutralization. All living ...

Amid a challenging gene editing climate, partnerships between researchers, regulators, and industry remain crucial for ...

Quantum-Si Customer to Showcase Protein Barcoding for Nucleic Acid–LNP Therapeutic Development at Festival of Genomics Boston ...

Japanese researchers have successfully eliminated the extra chromosome responsible for Down syndrome using CRISPR gene ...

Here comes the anti-CRISPR protein AcrVIB1, a promising inhibitor whose precise role has not yet been determined. In cooperation with the Helmholtz Centre for Infection Research (HZI) in ...

Designing proteins with the help of AI can boost R&D massively. Proteins can be designed to destroy PFAS, to remove the ...

Editas Medicine ( EDIT 12.04%) is a promising clinical-stage company that has captured Wall Street's attention at the ...

CRISPR Gene editing therapy is used for the first time in living humans with amazing results.

RNA gene scissors (CRISPR-Cas13) are gaining significant attention as a next-generation gene therapy with fewer side effects.

Researchers have created a standardized mouse stem cell library containing 63 genetic variants strongly linked to autism ...

Delve into what the new CRISPR tool, CAST, has to offer. CRISPR-associated transposases are already gaining traction in ...